The structure of human interferon- ? : implications for activity

Interferons (IFNs) are potent extracellular protein mediators of host defence and homoeostasis. This article reviews the structure of human IFN-β (HuIFN-β), in particular in relation to its activity. The recently determined crystal structure of HuIFN-β provides a framework for understanding of the m...

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Veröffentlicht in:Cellular and molecular life sciences : CMLS 1998-11, Vol.54 (11), p.1203-1216
Hauptverfasser: Karpusas, M., Whitty, A., Runkel, L., Hochman, P.
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Sprache:eng
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Zusammenfassung:Interferons (IFNs) are potent extracellular protein mediators of host defence and homoeostasis. This article reviews the structure of human IFN-β (HuIFN-β), in particular in relation to its activity. The recently determined crystal structure of HuIFN-β provides a framework for understanding of the mechanism of differentiation of type I IFNs by their common receptor. Insights are generated by comparison with the structures of other type I IFNs and from the interpretation of existing mutagenesis data. The details of the observed carbohydrate structure, together with biochemical data, implicate the glycosylation of HuIFN-β, which is uncommon among type I IFNs, as an important factor in the solubility, stability and, consequently, activity of the protein. Finally, these structural implications are discussed in the context of the clinical use of HuIFN-β.[PUBLICATION ABSTRACT]
ISSN:1420-682X
1420-9071
DOI:10.1007/s000180050248